Journal article
A multicentre randomized trial of the treatment of patients with pemphigus vulgaris with infliximab and prednisone compared with prednisone alone
British journal of dermatology (1951), Vol.172(3), pp.760-768
03/01/2015
DOI: 10.1111/bjd.13350
PMCID: PMC4326612
PMID: 25123295
Abstract
Background Pemphigus vulgaris (PV) is a blistering disease and tumour necrosis factor-alpha has a role in its pathogenesis.
Objectives To evaluate the safety of infliximab (IFX) with prednisone compared with prednisone alone in the treatment of PV. In addition, treatment response was assessed and mechanistic studies were performed.
Methods Subjects with PV who had ongoing disease activity while being maintained on prednisone were randomized to receive either IFX or placebo in addition to prednisone. Response status and immunoglobulin (Ig) G anti-desmoglein (Dsg) 1 and Dsg3 antibodies were assessed at 18 and 26 weeks.
Results Ten subjects were randomized to each group. There were no safety signals during the course of the study. At week 18, one subject in each group had responded. At week 26, three IFX-treated subjects vs. none in the placebo group had responded (P = 0.21). At weeks 18 and 26, the median IgG anti-Dsg1 and anti-Dsg3 levels were lower in the IFX-treated patients [IgG anti-Dsg-1 (week 18, P = 0.035; week 26, P = 0.022); IgG anti-Dsg3 (week 18, P = 0.035; week, 26 P = 0.05)].
Conclusions This study is limited by the relatively small sample size. There was no significant difference between study arms in the proportion of subjects with treatment-related adverse events > grade 3. IFX therapy was not shown to be effective for the treatment of patients with PV in this randomized, placebo-controlled trial, although IFX treatment may be associated with a decrease in anti-Dsg1 and Dsg3 antibodies.
Details
- Title: Subtitle
- A multicentre randomized trial of the treatment of patients with pemphigus vulgaris with infliximab and prednisone compared with prednisone alone
- Creators
- R. P. Hall - Duke UniversityJ. Fairley - University of IowaD. Woodley - University of Southern CaliforniaV. P. Werth - University of PennsylvaniaD. Hannah - Duke UniversityR. D. Streilein - Duke UniversityJ. McKillip - University of IowaJ. Okawa - University of PennsylvaniaM. Rose - University of PennsylvaniaL. L. Keyes-Elstein - Rho (United States)A. Pinckney - Rho (United States)A. Overington - Rho (United States)J. Wedgwood - National Institute of Allergy and Infectious DiseasesL. Ding - National Institute of Allergy and Infectious DiseasesB. Welch - National Institute of Allergy and Infectious Diseases
- Resource Type
- Journal article
- Publication Details
- British journal of dermatology (1951), Vol.172(3), pp.760-768
- DOI
- 10.1111/bjd.13350
- PMID
- 25123295
- PMCID
- PMC4326612
- NLM abbreviation
- Br J Dermatol
- ISSN
- 0007-0963
- eISSN
- 1365-2133
- Publisher
- Wiley
- Number of pages
- 9
- Grant note
- U19AI056363 / NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Allergy & Infectious Diseases (NIAID) 5U19AI056363-7 / Autoimmunity Centers of Excellence, NIAID
- Language
- English
- Date published
- 03/01/2015
- Academic Unit
- Dermatology
- Record Identifier
- 9984296306102771
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